K-number	K910768
Device name	SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE
Applicant	Surgitek Medical Engineering Corp.
Product code	FGE
Device class	Class II
Decision date	Mar 19, 1991
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE

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